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Dietary intervention in the management of phenylketonuria: current perspectives
Phenylketonuria (PKU) is a well-described inborn error of amino acid metabolism that has been treated for >60 years. Enzyme deficiency causes accumulation of phenylalanine (Phe) and if left untreated will lead to profound and irreversible intellectual disability in most children. Traditionally, i...
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| Publicado no: | Pediatric Health Med Ther |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5683291/ https://ncbi.nlm.nih.gov/pubmed/29388626 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PHMT.S49329 |
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